45776
二苯并噻吩
analytical standard
别名:
DBT, 二苯噻吩
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关于此项目
经验公式（希尔记法）:
C12H8S
化学文摘社编号:
分子量:
184.26
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-072-9
Beilstein/REAXYS Number:
121101
MDL number:
产品名称
二苯并噻吩, analytical standard
InChI key
IYYZUPMFVPLQIF-UHFFFAOYSA-N
InChI
1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H
SMILES string
c1ccc2c(c1)sc3ccccc23
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
bp
332-333 °C (lit.)
mp
97-100 °C (lit.)
application(s)
environmental
format
neat
Quality Level
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
338.0 °F
flash_point_c
170 °C
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
A Stephen K Hashmi et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(21), 6576-6580 (2012-04-21)
With the IPr ligand (IPr=1,3-bis-(2,6-diisopropylphenyl)imidazol-2-ylidene) on gold(I) excellent yields in the benzanellation of 2-substituted thiophenes, benzothiophenes, pyrroles, benzofurans, and indoles were achieved. The 1-siloxybut-3-ynyl side chains, incorporated in the anellation, are easily accessible by the addition of a propargyl metal
Mykola Seredych et al.
ChemSusChem, 4(1), 139-147 (2011-01-13)
Adsorption of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (DMDBT) from simulated diesel fuel was investigated with polymer-derived carbon matrices. Sulfur was incorporated to the carbon surface via a high-temperature hydrogen sulfide reduction of oxygen-containing groups. The resultant carbons were characterized by nitrogen
Santhosh Reddy Patpi et al.
Journal of medicinal chemistry, 55(8), 3911-3922 (2012-03-28)
A molecular hybridization approach is an emerging structural modification tool to design new molecules with improved pharmacophoric properties. In this study, 1,2,3-triazole-based Mycobacterium tuberculosis inhibitors and synthetic and natural product-based tricyclic (carbazole, dibenzo[b,d]furan, and dibenzo[b,d]thiophene) antimycobacterial agents were integrated in
Adeniyi S Ogunlaja et al.
Dalton transactions (Cambridge, England : 2003), 41(45), 13908-13918 (2012-10-02)
The reaction between [V(IV)OSO(4)] and the tetradentate N(2)O(2)-donor Schiff base ligand, N,N-bis(o-hydroxybenzaldehyde)phenylenediamine (sal-HBPD), obtained by the condensation of salicylaldehyde and o-phenylenediamine in a molar ratio of 2 : 1 respectively, resulted in the formation of [V(IV)O(sal-HBPD)]. The molecular structure of
Palladium-catalyzed double C-H activation directed by sulfoxides in the synthesis of dibenzothiophenes.
Rajarshi Samanta et al.
Angewandte Chemie (International ed. in English), 50(22), 5217-5220 (2011-04-21)
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